Figure 2
Uncommonly observed but characteristic genotype-phenotype correlations. Retinal phenotype associated with mutations in CRB1 [#117] (A), KIF11 [#179] (B), JAG1 [#184] (C), DRAM2 [#119] (D), POC1B [#120] (E), NPHP1 [#115] (F), RPGR [#189] (G). Fundus color image (first column), fundus AF with 488 nm excitation light (second column), and horizontal spectral-domain OCT (third and fourth column) are shown. Patient numbers refer to Supplementary Table 1. Only one eye is shown due to high symmetry between eyes.
